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FDA 510(k)

IPL Hair Remover, Model: G993, G996, G998 and G885

K-Number: K211368 · 2021-10-04

ApplicantShenzhen Mywin Technology Co., Ltd.
Decision Date2021-10-04
Product CodeONF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IPL Hair Remover, Model: G993, G996, G998 and G885 is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Mywin Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-10-04 under 510(k) number K211368. The device is classified under product code ONF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPL Hair Remover, Model: G993, G996, G998 and G885?

IPL Hair Remover, Model: G993, G996, G998 and G885 is a medical device that received FDA 510(k) clearance on 2021-10-04. The listed applicant is Shenzhen Mywin Technology Co., Ltd.. The 510(k) number is K211368.

When did IPL Hair Remover, Model: G993, G996, G998 and G885 receive FDA 510(k) clearance?

IPL Hair Remover, Model: G993, G996, G998 and G885 received FDA 510(k) clearance on 2021-10-04, under 510(k) number K211368.

Who is the listed applicant for IPL Hair Remover, Model: G993, G996, G998 and G885?

The FDA 510(k) record lists Shenzhen Mywin Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IPL Hair Remover, Model: G993, G996, G998 and G885?

The FDA product code for IPL Hair Remover, Model: G993, G996, G998 and G885 is ONF.

Other records listing Shenzhen Mywin Technology Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K221679IPL Hair Remover, Model: G993, G996, G998 and G885

Related Devices (Code: ONF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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